BEUDAMED
    26 results · 24ms · Sources: EU EUDAMED, US FDA

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    Actreen Hi-Lite Cath, Actreen Hi-Lite Set

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    NITREX™

    FDA UDI
    EV3, INC·00763000185398·GW N180801 NITREX V04

    NITREX

    FDA UDI
    Covidien LP·10821684009038·Guidewire

    NITREX

    FDA UDI
    Covidien LP·00821684058152·Guidewire

    Ophthalmic Retractor

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100943·JAFFE LID RETRACTOR SMALL

    Origin Hip Stem

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215053345·

    n/a

    FDA UDI
    Ortho Development Corporation·00822409067596·Stem Extension Trial Diameter 18x80mm

    eTRAX™ Needle

    FDA UDI
    CIVCO MEDICAL INSTRUMENTS CO., INC.·00841436103466·Sterile needle, 18GA x 8cm with (7.6 tapered to...

    Origin

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215007812·

    PUMA MODEL VERSION 1.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    WV3000T DIGITAL X-RAY DIRECT IMAGING FLAT PANEL DETECTOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    NITREX

    FDA Adverse Event
    Malfunction ·EV3, INC.·Product code DQX·June 26, 2023

    ASR UNI FEMORAL IMPL SIZE 41

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·June 20, 2013

    PILLING HEPARIN CANNULA 1.5MM TIP 2 1/8"

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code DWF·April 29, 2011

    SILICONE ADVANCED OPTIC LENS

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·September 23, 2008

    AMC/3 ARTERIAL NEEDLE 21GA X 1

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES·Product code GDF·July 12, 2023

    1823260-2015-04202

    FDA Adverse Event
    Malfunction ·September 22, 2015

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·April 19, 2019

    CARCINOEMBRYONIC ANTIGEN - CEA

    FDA Adverse Event
    Malfunction ·ROCHE DIAGOSTICS·Product code DHX·December 21, 2015

    VIDAS® TOXO IGG II

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code LGD·February 16, 2018